Variant report
Variant | rs13032365 |
---|---|
Chromosome Location | chr2:115988211-115988212 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12616332 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12616456 | 0.92[ASN][1000 genomes] |
rs12617588 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12619497 | 0.91[ASN][1000 genomes] |
rs12619606 | 0.92[ASN][1000 genomes] |
rs12624162 | 0.99[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12991665 | 0.93[ASN][1000 genomes] |
rs12993170 | 0.92[ASN][1000 genomes] |
rs12998960 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs13001269 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13005061 | 1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs13007061 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs13009552 | 0.92[ASN][1000 genomes] |
rs13011541 | 0.93[ASN][1000 genomes] |
rs13031722 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs35363264 | 0.84[ASN][1000 genomes] |
rs35672000 | 0.84[ASN][1000 genomes] |
rs35747327 | 1.00[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs4399739 | 0.92[ASN][1000 genomes] |
rs71418540 | 0.92[ASN][1000 genomes] |
rs71418546 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1014713 | chr2:115858427-116018055 | Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv1001542 | chr2:115920847-116082585 | Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv834339 | chr2:115953298-116132979 | Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv522754 | chr2:115983419-116003178 | Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding region | 1 gene(s) | inside rSNPs | diseases |
No data |